HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-bromobutanimide → Ethyl 5-bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Ethyl 8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylate | HCID 14207617 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 5-bromo-8-morpholinoimidazo[1,2-a]pyrazine-2-carboxylate | HCID 117727933 | — |
Reaction Steps
To a solution of compound 1c (3.2 g, 9.0 mmol) in DCM (100 mL) at 0° C. was added NBS (1.6 g, 9.0 mmol) portionwise. The reaction mixture was allowed to stir at rt for 10 min, and subsequently was washed with a saturated aqueous sodium bicarbonate (2×100 mL). The organic layer was separated, dried over Na2SO4 and concentrated under reduced pressure to give compound 21a as an off-white solid. Mass Spectrum (LCMS, ESI pos.) Calcd. For C13H15BrN4O3: 356.2 (M+H). Found 356.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09249163B2 |
| Source dataset | uspto-grants-2016_02 |
| ORD ID | ord-cde9cdc915ac4fc3828daca598e78800 |
| Source note | uspto-grants-2016_02 |